Category: 216961-61-4

2-Sep-21 News Simple exploration of 216961-61-4

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, tert-Butyl (10-aminodecyl)carbamate, other downstream synthetic routes, hurry up and to see.

Related Products of 216961-61-4, The chemical industry reduces the impact on the environment during synthesis 216961-61-4, name is tert-Butyl (10-aminodecyl)carbamate, I believe this compound will play a more active role in future production and life.

General procedure 2. Starting compound III: S-Methyl N-cyano-N’-(2-methyl4-pyridylisothiourea. Starting compound IV: 10-t-Butoxycarbonylaminodecylamine. Purification: Flash chromatography (Eluent 1% NH3(aq) and 0-10% MeOH in CH2Cl2). The compound was obtained as a yellow oil. 13C NMR (CDCl3) delta: 158.1, 157.3, 155.5, 149.4, 146.2, 116.5, 113.5, 112.0, 77.2, 41.7, 29.4, 28.9, 28.8, 28.6, 28.6, 28.6, 28.2, 26.2, 26.1, 24.0.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, tert-Butyl (10-aminodecyl)carbamate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Leo Pharmaceutical Products, Ltd. A/S; US6346520; (2002); B1;,
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Some tips on 216961-61-4

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route tert-Butyl (10-aminodecyl)carbamate, its application will become more common.

Related Products of 216961-61-4,Some common heterocyclic compound, 216961-61-4, name is tert-Butyl (10-aminodecyl)carbamate, molecular formula is C15H32N2O2, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

General procedure 2. Starting compound III: S-Methyl N-cyano-N-(2-methoxy-5-pyridylisothiourea. Starting compound IV: 10-t-Butoxycarbonylaminodecylamine. Purification: Flash chromatography (Eluent 1% NH3(aq) and 0-6% MeOH in CH2Cl2) and crystallization from ether. 13C NMR (CDCl3) delta: 161.2, 158.6, 155.5, 143.3, 137.0, 127.9, 117.3, 110.3, 77.2, 53.2, 41.3, 29.4, 28.9, 28.8, 28.8, 28.6, 28.6, 28.2, 26.2, 26.1

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route tert-Butyl (10-aminodecyl)carbamate, its application will become more common.

Reference:
Patent; Leo Pharmaceutical Products, Ltd. A/S; US6346520; (2002); B1;,
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics