Hydrochloric Acid → HCID 178439171, compound

HRID 602243Notes

Reaction equation

HRID 602243 reaction equation
[CH2:1]([C:4]1[N:8]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[C:22]3[N:26](C(C4C=CC=CC=4)(C4C=CC=CC=4)C4C=CC=CC=4)[N:25]=[N:24][N:23]=3)=[CH:12][CH:11]=2)[C:7]([CH:46]=[O:47])=[CH:6][CH:5]=1)[CH2:2][CH3:3].Cl>>[CH2:1]([C:4]1[N:8]([CH2:9][C:10]2[CH:11]=[CH:12][C:13]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[C:22]3[NH:23][N:24]=[N:25][N:26]=3)=[CH:14][CH:15]=2)[C:7]([CH:46]=[O:47])=[CH:6][CH:5]=1)[CH2:2][CH3:3]

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 14987391HCID 14987391, compound

Product 1

HCID 178439171HCID 178439171, compoundYield 71%

Procedure

This compound was prepared using the same procedure as in Example 1.15 g of 5-n-propyl-1-[2′-(1-triphenylmethyltetrazol-5-yl)biphenyl-4-yl-methyl]-2-pyrrolaldehyde (0.024 moles) and 30 mL of 4N HCl (0.120 moles) yield 6.3 g of product. Formula: C22H21N5O (m.w. 371.44). Yield 71%.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-eac1c4fae1dd42e7831b158ee0e3150b
Source dataset
uspto-grants-2011_03
Patent number
US07906501B2

Reaction notes

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