7-Aminoheptanoic acid → HCID 178525426, compound

HRID 27139

Reaction equation

HRID 27139 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9].[NH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([OH:22])=[O:21].NCCCCCCCCCCC(O)=O.C([NH:40][C:41](=[S:44])[S:42]C)(O)=O.[N-:45]=[N+:46]=[N-:47].[Na+]>>[C:8]([CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][N:1]1[C:41]([SH:44])=[N:40][N:46]=[N:45]1)([OH:10])=[O:9].[C:20]([CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][N:11]1[C:41]([SH:42])=[N:47][N:46]=[N:45]1)([OH:22])=[O:21]

Participants

7

Procedure

When 7-aminoheptanoic acid or 9-aminononanoic acid is substituted in the procedure of Example 19 in place of 11-aminoundecanoic acid and the resulting methyl carboxydithiocarbamate is treated with sodium azide as described therein, 1-(6-carboxyhexyl)tetrazole-5-thiol and 1-(8-carboxyoctyl)tetrazole-5-thiol are obtained, respectively.

Sources & evidence

ORD record
ord-03318d54ecce4d5e86c676160360730b
Source dataset
uspto-grants-1980_09
Patent number
US04220644

Linked notes

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